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FDA 510(k)

JSA REPROCESSED COMPRESSION SLEEVE DEVICES

K-Number: K031722 · 2003-11-25

Decision Date2003-11-25
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

JSA REPROCESSED COMPRESSION SLEEVE DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is Jack Speer and Assoc., Inc.. It received FDA 510(k) clearance on 2003-11-25 under 510(k) number K031722. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JSA REPROCESSED COMPRESSION SLEEVE DEVICES?

JSA REPROCESSED COMPRESSION SLEEVE DEVICES is a medical device that received FDA 510(k) clearance on 2003-11-25. The listed applicant is Jack Speer and Assoc., Inc.. The 510(k) number is K031722.

When did JSA REPROCESSED COMPRESSION SLEEVE DEVICES receive FDA 510(k) clearance?

JSA REPROCESSED COMPRESSION SLEEVE DEVICES received FDA 510(k) clearance on 2003-11-25, under 510(k) number K031722.

Who is the listed applicant for JSA REPROCESSED COMPRESSION SLEEVE DEVICES?

The FDA 510(k) record lists Jack Speer and Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JSA REPROCESSED COMPRESSION SLEEVE DEVICES?

The FDA product code for JSA REPROCESSED COMPRESSION SLEEVE DEVICES is JOW.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Jack Speer and Assoc., Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: JOW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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